chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145341851145341852GA25GENIChomozygous112870784
4145343247145343248GA22GENIChomozygous112870786
4145345010145345011TC10GENIChomozygous112870788
4145347173145347174CT12GENIChomozygous112870789
4145348527145348528AG2GENIChomozygous112870790
4145349663145349664GA15GENIChomozygous112870796
4145350121145350122AT25GENIChomozygous112870797
4145350671145350672CT16GENIChomozygous112870798
4145351090145351091CT18GENIChomozygous112870799
4145354146145354147GC15GENIChomozygous112870800
4145354549145354550GA16GENIChomozygous112870801
4145354894145354895CT26GENIChomozygous112870803
4145355614145355615AG13GENIChomozygous112870804
4145356361145356362AC19GENIChomozygous112870805
4145356418145356419TC22GENIChomozygous112870806
4145356424145356425GA23GENIChomozygous112870807
4145356960145356961AT15GENIChomozygous112870808
4145357076145357077TC14GENIChomozygous112870809
4145357179145357180GC19GENIChomozygous112870810
4145357360145357361TA16GENIChomozygous112870811
4145358592145358593CT8GENIChomozygous112870812
4145358919145358920TC13GENIChomozygous112870813
4145359534145359535AG13GENIChomozygous112870814
4145359628145359629TG24GENIChomozygous112870815
4145361065145361066AG8GENIChomozygous112870816
4145362996145362997CT10GENIChomozygous112870817
4145363773145363774CT13GENIChomozygous112870818
4145364439145364440TC9GENIChomozygous112870819
4145364702145364703CT15GENIChomozygous112870820